Carbonation reactivity of wollastonite enhanced by incorporating sodium-based alkali additives

The carbonation of wollastonite presents a promising approach for CO 2 sequestration and the development of sustainable cementitious materials. This study investigates the enhancement of wollastonite carbonation through the incorporation of sodium-based additives (Na 2 CO 3 and NaHCO 3 ) under carbonation curing conditions. X-ray diffraction analysis revealed that increasing the dosage of Na₂CO₃ and NaHCO₃ facilitated wollastonite dissolution and promoted calcite formation. Thermogravimetric analysis confirmed that bound CO 2 content was significantly high in carbonated samples, especially when containing NaHCO 3 at dosages of 3%. Thermodynamic modeling further indicated that wollastonite carbonation led to the formation of calcium-silicate-hydrate alongside minor phases such as magnesium-silicate-hydrate and hydrotalcite. These findings suggest that sodium-based alkali additives are an effective promoter of wollastonite dissolution and carbonation, enhancing CO 2 sequestration efficiency and contributing to the development of low-carbon cementitious materials. • Sodium-based additives (Na 2 CO 3 and NaHCO 3 ) enhance wollastonite carbonation reactivity. • NaHCO 3 is more effective than Na 2 CO 3 in promoting wollastonite dissolution. • A 3% NaHCO 3 dosage yields the highest CO 2 uptake. • Calcite and C-S-H are the main products of accelerated wollastonite carbonation. • Thermodynamic modeling confirms increased C-S-H and calcite with additives.

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Publication Details

Journal
Journal of CO2 Utilization
Published
2026-03-09
DOI
https://doi.org/10.1016/j.jcou.2026.103378
Primary Topic
CO2 Sequestration and Geologic Interactions
Type
article
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article

Carbonation reactivity of wollastonite enhanced by incorporating sodium-based alkali additives

J.T. Kim, Melaku N. Seifu, Seunghee Park, Solmoi Park et al.
Journal of CO2 Utilization
CO2 Sequestration and Geologic Interactions
article

Carbonation reactivity of wollastonite enhanced by incorporating sodium-based alkali additives

J.T. Kim, Melaku N. Seifu, Seunghee Park, Solmoi Park, Seonhyeok Kim
article en

Abstract

The carbonation of wollastonite presents a promising approach for CO 2 sequestration and the development of sustainable cementitious materials. This study investigates the enhancement of wollastonite carbonation through the incorporation of sodium-based additives (Na 2 CO 3 and NaHCO 3 ) under carbonation curing conditions. X-ray diffraction analysis revealed that increasing the dosage of Na₂CO₃ and NaHCO₃ facilitated wollastonite dissolution and promoted calcite formation. Thermogravimetric analysis confirmed that bound CO 2 content was significantly high in carbonated samples, especially when containing NaHCO 3 at dosages of 3%. Thermodynamic modeling further indicated that wollastonite carbonation led to the formation of calcium-silicate-hydrate alongside minor phases such as magnesium-silicate-hydrate and hydrotalcite. These findings suggest that sodium-based alkali additives are an effective promoter of wollastonite dissolution and carbonation, enhancing CO 2 sequestration efficiency and contributing to the development of low-carbon cementitious materials. • Sodium-based additives (Na 2 CO 3 and NaHCO 3 ) enhance wollastonite carbonation reactivity. • NaHCO 3 is more effective than Na 2 CO 3 in promoting wollastonite dissolution. • A 3% NaHCO 3 dosage yields the highest CO 2 uptake. • Calcite and C-S-H are the main products of accelerated wollastonite carbonation. • Thermodynamic modeling confirms increased C-S-H and calcite with additives.

Journal of CO2 UtilizationVol. 106
Korea Advanced Institute of Science and Technology (KR), Sungkyunkwan University (KR), Pukyong National University (KR)
Industry, innovation and infrastructure
Openalex Percentile: Top 38%
CO2 Sequestration and Geologic Interactions
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Carbonation reactivity of wollastonite enhanced by incorporating sodium-based alkali additives — J.T. Kim, Melaku N. Seifu, et al. · Journal of CO2 Utilization (2026) | TGRS Research Map | TGRS